Clinical Research Program Lead

2200 The Brigham and Women's Hospital, Inc.; Boston (MA); On-site; USD 79,000 - 129,000; Full time

Job summary

The Brigham and Women’s Hospital, Inc. (Mass General Brigham) is seeking a full-time Clinical Research Program Manager for the CARE program.

You will partner with investigators and clinicians to manage day-to-day operations, develop study protocols, and support manuscripts, abstracts, and grant proposals across local and national sites. The role includes staffing onboarding, regulatory compliance, and coordinating multi-site activities to advance cancer and well-being research.

Qualifications

• BA/BS degree required.
• Minimum of 2 years of management experience required.

Responsibilities

• Collaborate with the principal investigator to oversee all laboratory projects.
• Assist with grant submissions, including summarizing instructions and required elements, and collecting documentation.
• Assist with manuscript preparation for peer‑reviewed journals and submitting abstracts.
• Assist with abstract and presentation submissions for conferences at multiple levels.
• Write study protocols, IRB applications, informed consent documents, and manage timelines and amendments.
• Develop SOPs and templates to improve efficiency and consistency across studies.
• Oversee IRB communications and monitor clinical trial progress against milestones.
• Coordinate data collection and audits with various institutions and boards.

Skills

Management experience

Research coordination

Grant submissions

Manuscript preparation

IRB knowledge

Proposal writing

Education

BA/BS degree

Master’s degree or PhD preferred

Job description

The Brigham and Women’s Hospital, Inc. (Mass General Brigham) is seeking a full-time Clinical Research Program Manager for the CARE program.

You will partner with investigators and clinicians to manage day-to-day operations, develop study protocols, and support manuscripts, abstracts, and grant proposals across local and national sites. The role includes staffing onboarding, regulatory compliance, and coordinating multi-site activities to advance cancer and well-being research.